3-Hydroxylysine, a potential marker for studying radical-induced protein oxidation

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3-Hydroxylysine, a potential marker for studying radical-induced protein oxidation. / Morin, B; Bubb, W A; Davies, Michael Jonathan; Dean, R T; Fu, S.

In: Chemical Research in Toxicology, Vol. 11, No. 11, 11.1998, p. 1265-73.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Morin, B, Bubb, WA, Davies, MJ, Dean, RT & Fu, S 1998, '3-Hydroxylysine, a potential marker for studying radical-induced protein oxidation', Chemical Research in Toxicology, vol. 11, no. 11, pp. 1265-73. https://doi.org/10.1021/tx980118h

APA

Morin, B., Bubb, W. A., Davies, M. J., Dean, R. T., & Fu, S. (1998). 3-Hydroxylysine, a potential marker for studying radical-induced protein oxidation. Chemical Research in Toxicology, 11(11), 1265-73. https://doi.org/10.1021/tx980118h

Vancouver

Morin B, Bubb WA, Davies MJ, Dean RT, Fu S. 3-Hydroxylysine, a potential marker for studying radical-induced protein oxidation. Chemical Research in Toxicology. 1998 Nov;11(11):1265-73. https://doi.org/10.1021/tx980118h

Author

Morin, B ; Bubb, W A ; Davies, Michael Jonathan ; Dean, R T ; Fu, S. / 3-Hydroxylysine, a potential marker for studying radical-induced protein oxidation. In: Chemical Research in Toxicology. 1998 ; Vol. 11, No. 11. pp. 1265-73.

Bibtex

@article{f1cca97932c949e9beb86b4cff1d971f,
title = "3-Hydroxylysine, a potential marker for studying radical-induced protein oxidation",
abstract = "gamma-Irradiation of several amino acids (Val, Leu, Ile, Lys, Pro, and Glu) in the presence of O2 generates hydroperoxides. We have previously isolated and characterized valine and leucine hydroperoxides, and hydroxides, and have detected these products in both isolated systems [e.g., bovine serum albumin (BSA) and human low-density lipoprotein (LDL)] and diseased human tissues (atherosclerotic plaques and lens cataractous proteins). This work was aimed at investigating oxidized lysine as a sensitive marker for protein oxidation, as such residues are present on protein surfaces, and are therefore likely to be particularly susceptible to oxidation by radicals in bulk solution. HO* attack on lysine in the presence of oxygen, followed by NaBH4 reduction, is shown to give rise to (2S)-3-hydroxylysine [(2S)-2,6-diamino-3-hydroxyhexanoic acid], (2S)-4-hydroxylysine [(2S)-2,6-diamino-4-hydroxyhexanoic acid], (2S, 5R)-5-hydroxylysine [(2S,5R)-2,6-diamino-5-hydroxyhexanoic acid], and (2S,5S)-5-hydroxylysine [(2S,5S)-2,6-diamino-5-hydroxyhexanoic acid]. 5-Hydroxylysines are natural products formed by lysyl oxidase and are therefore not good markers of radical-mediated oxidation. The other hydroxylysines are however useful markers, with HPLC analysis of 9-fluorenylmethyl chloroformate (FMOC) derivatives providing a sensitive and accurate method for quantitative measurement. Hydroxylysines have been detected in the hydrolysates of peptides (Gly-Lys-Gly and Lys-Val-Ile-Leu-Phe) and proteins (BSA and histone H1) exposed to HO./O2, and subsequently treated with NaBH4. Quantification of the hydroxylysines yields, and comparison with hydroxyvalines and hydroxyleucines, supports the hypothesis that surface residues give higher yields of oxidized products than the hydrophobic leucines and valines, at least with globular proteins such as BSA. Hydroxylysines, and particularly 3-hydroxylysine, may therefore be sensitive and useful markers of radical-mediated protein oxidation in biological systems.",
keywords = "Amino Acids, Animals, Biological Markers, Cattle, Chromatography, High Pressure Liquid, Fluorenes, Free Radicals, Gamma Rays, Humans, Hydroxylysine, Mass Spectrometry, Oxidation-Reduction, Peptides, Proteins, Solvents",
author = "B Morin and Bubb, {W A} and Davies, {Michael Jonathan} and Dean, {R T} and S Fu",
year = "1998",
month = nov,
doi = "10.1021/tx980118h",
language = "English",
volume = "11",
pages = "1265--73",
journal = "Chemical Research in Toxicology",
issn = "0893-228X",
publisher = "American Chemical Society",
number = "11",

}

RIS

TY - JOUR

T1 - 3-Hydroxylysine, a potential marker for studying radical-induced protein oxidation

AU - Morin, B

AU - Bubb, W A

AU - Davies, Michael Jonathan

AU - Dean, R T

AU - Fu, S

PY - 1998/11

Y1 - 1998/11

N2 - gamma-Irradiation of several amino acids (Val, Leu, Ile, Lys, Pro, and Glu) in the presence of O2 generates hydroperoxides. We have previously isolated and characterized valine and leucine hydroperoxides, and hydroxides, and have detected these products in both isolated systems [e.g., bovine serum albumin (BSA) and human low-density lipoprotein (LDL)] and diseased human tissues (atherosclerotic plaques and lens cataractous proteins). This work was aimed at investigating oxidized lysine as a sensitive marker for protein oxidation, as such residues are present on protein surfaces, and are therefore likely to be particularly susceptible to oxidation by radicals in bulk solution. HO* attack on lysine in the presence of oxygen, followed by NaBH4 reduction, is shown to give rise to (2S)-3-hydroxylysine [(2S)-2,6-diamino-3-hydroxyhexanoic acid], (2S)-4-hydroxylysine [(2S)-2,6-diamino-4-hydroxyhexanoic acid], (2S, 5R)-5-hydroxylysine [(2S,5R)-2,6-diamino-5-hydroxyhexanoic acid], and (2S,5S)-5-hydroxylysine [(2S,5S)-2,6-diamino-5-hydroxyhexanoic acid]. 5-Hydroxylysines are natural products formed by lysyl oxidase and are therefore not good markers of radical-mediated oxidation. The other hydroxylysines are however useful markers, with HPLC analysis of 9-fluorenylmethyl chloroformate (FMOC) derivatives providing a sensitive and accurate method for quantitative measurement. Hydroxylysines have been detected in the hydrolysates of peptides (Gly-Lys-Gly and Lys-Val-Ile-Leu-Phe) and proteins (BSA and histone H1) exposed to HO./O2, and subsequently treated with NaBH4. Quantification of the hydroxylysines yields, and comparison with hydroxyvalines and hydroxyleucines, supports the hypothesis that surface residues give higher yields of oxidized products than the hydrophobic leucines and valines, at least with globular proteins such as BSA. Hydroxylysines, and particularly 3-hydroxylysine, may therefore be sensitive and useful markers of radical-mediated protein oxidation in biological systems.

AB - gamma-Irradiation of several amino acids (Val, Leu, Ile, Lys, Pro, and Glu) in the presence of O2 generates hydroperoxides. We have previously isolated and characterized valine and leucine hydroperoxides, and hydroxides, and have detected these products in both isolated systems [e.g., bovine serum albumin (BSA) and human low-density lipoprotein (LDL)] and diseased human tissues (atherosclerotic plaques and lens cataractous proteins). This work was aimed at investigating oxidized lysine as a sensitive marker for protein oxidation, as such residues are present on protein surfaces, and are therefore likely to be particularly susceptible to oxidation by radicals in bulk solution. HO* attack on lysine in the presence of oxygen, followed by NaBH4 reduction, is shown to give rise to (2S)-3-hydroxylysine [(2S)-2,6-diamino-3-hydroxyhexanoic acid], (2S)-4-hydroxylysine [(2S)-2,6-diamino-4-hydroxyhexanoic acid], (2S, 5R)-5-hydroxylysine [(2S,5R)-2,6-diamino-5-hydroxyhexanoic acid], and (2S,5S)-5-hydroxylysine [(2S,5S)-2,6-diamino-5-hydroxyhexanoic acid]. 5-Hydroxylysines are natural products formed by lysyl oxidase and are therefore not good markers of radical-mediated oxidation. The other hydroxylysines are however useful markers, with HPLC analysis of 9-fluorenylmethyl chloroformate (FMOC) derivatives providing a sensitive and accurate method for quantitative measurement. Hydroxylysines have been detected in the hydrolysates of peptides (Gly-Lys-Gly and Lys-Val-Ile-Leu-Phe) and proteins (BSA and histone H1) exposed to HO./O2, and subsequently treated with NaBH4. Quantification of the hydroxylysines yields, and comparison with hydroxyvalines and hydroxyleucines, supports the hypothesis that surface residues give higher yields of oxidized products than the hydrophobic leucines and valines, at least with globular proteins such as BSA. Hydroxylysines, and particularly 3-hydroxylysine, may therefore be sensitive and useful markers of radical-mediated protein oxidation in biological systems.

KW - Amino Acids

KW - Animals

KW - Biological Markers

KW - Cattle

KW - Chromatography, High Pressure Liquid

KW - Fluorenes

KW - Free Radicals

KW - Gamma Rays

KW - Humans

KW - Hydroxylysine

KW - Mass Spectrometry

KW - Oxidation-Reduction

KW - Peptides

KW - Proteins

KW - Solvents

U2 - 10.1021/tx980118h

DO - 10.1021/tx980118h

M3 - Journal article

C2 - 9815186

VL - 11

SP - 1265

EP - 1273

JO - Chemical Research in Toxicology

JF - Chemical Research in Toxicology

SN - 0893-228X

IS - 11

ER -

ID: 138283317